Evaluation of Hospitalization for Anorexia Nervosa (EVALuation de l'Apport de l'HOSPITalisation Pour Anorexie Mentale : EVALHOSPITAM) (EVHAN)

Institut Mutualiste Montsouris

Status: Unknown

Conditions: Anorexia Nervosa

Treatments: Other: inpatient treatment

Study type: Observational

Funder types: Other

Identifiers

NCT00910169

ANR-0-JC0719-6328

PHRC AOM 06 020

Eudract: 2007 -A01110-53

Details and patient eligibility

About

The objective of this research is to evaluate the efficacy of five different in-patient treatment modalities and predictive factors of outcome for anorexia nervosa. The primary hypothesis is that the different treatment types impact outcome of patients at discharge from inpatient treatment and at one year follow-up, even after adjustment for confounding factors (age, length of illness, number of previous hospitalizations, clinical state at intake).

Full description

This study will evaluate global, psychiatric, somatic and psychosocial outcome for inpatients with anorexia nervosa through three evaluations (intake, discharge and one-year follow-up). The study will also consider five types of in-patient treatment in a naturalistic setting (i.e., patients will not be assigned to different treatment conditions; rather, we will study inpatient care as it exists today). The five treatment modalities to be studied are:

1. Discharge weight objectives.
2. The practice of a separation period.
3. The use of clear nutritional and dietary objectives (cognitive/behavioural).
4. The intensity of family involvement in treatment.
5. Stabilisation phase before ending inpatient treatment.

Enrollment: 300 estimated patients

Sex: All

Ages: 8 to 65 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• All patients who accept participation between 8 and 50 years old, consecutively hospitalized for a DSM IV diagnosis of Anorexia Nervosa in one of the departments participating in this research by necessity of physical condition (BMI < 15, rapid weight loss) or psychological condition
• Parents of participating patients still living with their parents who accept participation

Exclusion criteria

• Refusal of research
• Patients who do not speak French
• Patients with a related somatic illness (diabetes, Crohn's disease, metabolic illness)
• Patients not covered by social security health insurance

Trial design

300 participants in 1 patient group

inpatient treatment

Description:

naturalistic treatment no modification: observational study

Treatment:

Other: inpatient treatment